HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368141Generated: November 1, 2026
Sodium borohydride → HCID 178472351, compound
https://huagongshe.com/reaction/2368141
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178472350 | HCID 178472350 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178472351 | HCID 178472351 | 104% |
Reaction Steps
To a solution of 1-({trans-4-[6-(cyclopropylmethoxy)-1,3-benzoxazol-2-yl]cyclohexyl}oxy)propan-2-one (259 mg) in ethanol (5 mL) was added sodium borohydride (57 mg) under ice-cooling. The reaction mixture was stirred at 0° C. for 1 hr, and extracted with ethyl acetate and 1M hydrochloric acid. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (271 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703758B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-d7c7451cd7364109987354ffd1a4c7ef |
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| Source note | uspto-grants-2014_04 |
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